Investigator

Armin M Gamper

Associate Professor · University of Alberta, Oncology

Research Interests

AMGArmin M Gamper
Papers(1)
BAIRDA: a novel in vi…
Collaborators(5)
Braden ChowBrad WarkentinF. HuangGeetha MenonSunita Ghosh
Institutions(2)
University Of AlbertaCross Cancer Institute

Papers

BAIRDA: a novel in vitro setup to quantify radiobiological parameters for cervical cancer brachytherapy dose estimations

AbstractObjective. Brachytherapy (BT) dose prescriptions for locally advanced cervical cancer are made with account for the radiobiological parameters,α/βratio and halftime of repair (T1/2). However, a wide range of parameter values has been reported which can challenge commonly held equivalencies between dose prescriptions. This is the first reported study that aims to develop anin vitroexperimental technique using clinical high-dose-rate (HDR) and pulsed-dose-rate (PDR) Ir-192 brachytherapy afterloaders to quantify these parametersin vitroand to contextualize findings within contemporary practice.Approach. To efficiently quantifyα/βandT1/2,in vitroexperiments more reflective of clinical BT practice than traditional clonogenic survival assays were developed and applied to four squamous cell carcinoma cell lines (CaSki, C-33A, SiHa, and SW756). Radiation was delivered using single acute and fractionated dose treatments with a conventional irradiator and clinical HDR and PDR BT afterloaders. For the latter, a novelbrachytherapyafterloaderin vitroradiationdeliveryapparatus (BAIRDA) was developed.Main Results. Theα/βandT1/2values determined using BAIRDA and the conventional irradiator showed close agreement, validating the novel apparatus and technique. For CaSki, C-33A, SiHa, and SW756, the BAIRDA-measuredα/βratios (5.2 [4.6–5.8], 5.6 [4.5–6.6], 6.3 [4.9–7.7], and 5.3 [4.7–6.0] Gy, respectively) were consistently smaller, while theT1/2(3.3 [2.7–3.9], 2.7 [2.0–3.3], 2.8 (2.4–3.1], and 4.8 [4.1–5.4] hours) larger, than the widely accepted values in clinical practice (α/β= 10 Gy;T1/2 = 1.5 h).Significance.In vitroexperiments using BAIRDA provided evidence for differences between the conventionally selected and experimentally determinedα/βratio andT1/2. Treatment regimens using HDR-BT and PDR-BT, designed to deliver equivalent radiobiological doses based on conventional values, were shown to differ by up to 27 Gy EQD2 – an effect that could impact treatment outcomes in cervical cancer. Furthermore, with BAIRDA, we have developed a novel method for radiobiological research in BT.

33Works
1Papers
5Collaborators
Uterine Cervical NeoplasmsBreast NeoplasmsCell Line, TumorDisease-Free SurvivalDrug Resistance, NeoplasmXenograft Model Antitumor Assays

Positions

2015–

Associate Professor

University of Alberta · Oncology

2012–

research associate

University of Pittsburgh · Radiation Oncology

2008–

postdoctoral fellow

University of Pittsburgh · Cell Biology / Radiation Oncology

2006–

postdoctoral fellow

Rockefeller University · Molecular Biology and Biochemistry

Education

2006

Ph.D.

Rockefeller University · Biochemistry and Molecular Biology

1998

research assistant

Free University of Berlin · Biochemistry

1995

Mag. rer. nat.

University of Innsbruck · Chemistry

1994

Erasmus scholar

Universidade da Coruña · Chemistry

Country

CA